CS settled the mesocosm experiment and assisted in the samplings. EGB, MB, FP and AM conceived the idea and contributed in performing part of the analyses and in drafting the manuscript. All authors have given final approval Bafilomycin A1 supplier of the version to be published.”
“Background Yersinia pestis and Bacillus anthracis are two pathogens of significant concern to public health from a biodefense perspective [1, 2]. Y. pestis, the causative agent of plague, is a Gram-negative, highly communicable coccobacillus that has been responsible for three historic pandemics with high mortality rates [3–5]. The microorganism possesses a Type III secretion mechanism common to several

human, animal and plant pathogens, whereby a series of pathogen-specific structural proteins form a syringe-like structure capable of injecting virulence factors into the mammalian host cell.

These virulence factors then facilitate pathogen use of host nutrients and thwart the host immune response, ultimately causing cell and host death [6, 7]. Naturally occurring plague can be transmitted from infected fleas and rodents to humans, and although the pathogen can be phagocytosed, it can also resist destruction by manipulating the host defense mechanism(s), potentially GSK872 through antigenic mimicry [8]. Y. pestis then multiplies rapidly leading to necrosis of lymph nodes, a condition known LY2874455 ic50 as bubonic plague, which can result in death if untreated [2]. In some cases the infection can spread through the blood stream resulting in systemic plague (septicemia) or to the lungs resulting next in the highly contagious and deadly form of the disease known as pneumonic plague. There are currently no rapid, widely available diagnostic tests for plague, and the most common treatment is streptomycin [2,

3], an antibiotic with adverse effects. Two other species from the genus Yersinia are also human pathogens: Y. pseudotuberculosis and Y. enterocolitica[9, 10]. Despite their high degree of sequence similarity to Y. pestis, these two near neighbors of Y. pestis manifest in very different symptoms, ranging from abdominal pain to septicemia in humans, usually caused by infection through contaminated food. Infections caused by Y. pseudotuberculosis or Y. enterocolitica can be effectively treated with antibiotics and in most cases are self-limiting. Notably, Y. pestis is reported to have evolved from Y. pseudotuberculosis within the past 10,000 years [11]. B. anthracis is a Gram-positive, rod-shaped spore-forming bacterial pathogen and the causative agent of anthrax [12, 13]. Human, livestock, and wildlife mortalities attributable to anthrax occur in numerous regions of the world, although the majority of cases are found in less industrialized nations [14]. Three forms of the disease have been described: cutaneous, intestinal and inhalational.